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MR spectroscopy and diffusion tensor imaging of the brain in congenital muscular dystrophy with merosin deficiency: metabolite level decreases, fractional anisotropy decreases, and apparent diffusion coefficient increases in the white matter.
Sijens PE, Fock JM, Meiners LC, Potze JH, Irwan R, Oudkerk M. Sijens PE, et al. Among authors: fock jm. Brain Dev. 2007 Jun;29(5):317-21. doi: 10.1016/j.braindev.2006.10.004. Epub 2006 Nov 17. Brain Dev. 2007. PMID: 17113260
Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome.
O'Grady GL, Verschuuren C, Yuen M, Webster R, Menezes M, Fock JM, Pride N, Best HA, Benavides Damm T, Turner C, Lek M, Engel AG, North KN, Clarke NF, MacArthur DG, Kamsteeg EJ, Cooper ST. O'Grady GL, et al. Among authors: fock jm. Neurology. 2016 Oct 4;87(14):1442-1448. doi: 10.1212/WNL.0000000000003179. Epub 2016 Sep 2. Neurology. 2016. PMID: 27590285 Free PMC article.
Prevalence of Bladder and Bowel Dysfunction in Duchenne Muscular Dystrophy Using the Childhood Bladder and Bowel Dysfunction Questionnaire.
Lionarons JM, de Groot IJM, Fock JM, Klinkenberg S, Vrijens DMJ, Vreugdenhil ACE, Medici-van den Herik EG, Cuppen I, Jaeger B, Niks EH, Hoogerhuis R, Platte-van Attekum N, Feron FJM, Faber CG, Hendriksen JGM, Vles JSH. Lionarons JM, et al. Among authors: fock jm. Life (Basel). 2021 Jul 30;11(8):772. doi: 10.3390/life11080772. Life (Basel). 2021. PMID: 34440515 Free PMC article.
Mild axonal neuropathy of children during treatment for acute lymphoblastic leukaemia.
Reinders-Messelink HA, Van Weerden TW, Fock JM, Gidding CE, Vingerhoets HM, Schoemaker MM, Göeken LN, Bökkerink JP, Kamps WA. Reinders-Messelink HA, et al. Among authors: fock jm. Eur J Paediatr Neurol. 2000;4(5):225-33. doi: 10.1053/ejpn.1999.0310. Eur J Paediatr Neurol. 2000. PMID: 11030069 Clinical Trial.
39 results